Aripiprazole
- Product NDC
- 63187-965
- 11-digit product format
- 631870965
- Labeler code
- 63187
- Product ID
- 63187-965_3f575cc4-f92e-4e55-aeb2-c634fe3411d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA204838
- Marketing category
- ANDA
- Marketing start
- 2016-06-20
- Substance
- ARIPIPRAZOLE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 82VFR53I78 | ARIPIPRAZOLE | 129722-12-9 | ARIPIPRAZOLE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63187-965-30 | 63187096530 | 30 TABLET in 1 BOTTLE (63187-965-30) | 30 tablet | 2018-01-01 | No | No | Historical |
| 63187-965-60 | 63187096560 | 60 TABLET in 1 BOTTLE (63187-965-60) | 60 tablet | 2018-01-01 | No | No | Historical |
| 63187-965-90 | 63187096590 | 90 TABLET in 1 BOTTLE (63187-965-90) | 90 tablet | 2018-01-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Aripiprazole | Proficient Rx LP | 2019-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |